Canonical Allele Identifier: CA3181375149

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199494C= , CM000672.2:g.68199494C=	GRCh38
NC_000010.10:g.69959251C= , CM000672.1:g.69959251C=	GRCh37
NC_000010.9:g.69629257C=	NCBI36
NG_032118.1:g.98378C= , LRG_410:g.98378C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3412C= MANE Select	NP_115967.2:p.Gln1138=
ENST00000358913.10:c.3412C= MANE Select	ENSP00000351790.5:p.Gln1138=
NM_001256267.1:c.3412C=	NP_001243196.1:p.Gln1138=
NM_001256267.2:c.3412C=	NP_001243196.1:p.Gln1138=
NM_001256268.1:c.2530C=	NP_001243197.1:p.Gln844=
NM_001256268.2:c.2530C=	NP_001243197.1:p.Gln844=
NM_032578.3:c.3412C= , LRG_410t1:c.3412C=	NP_115967.2:p.Gln1138=
NR_045662.3:n.2839C=
NR_045662.4:n.2949C=
NR_045663.3:n.3541C=
NR_045663.4:n.3486C=
ENST00000354393.6:c.2587C=	ENSP00000346369.2:p.Gln863=
ENST00000354393.7:c.2587C=	ENSP00000346369.2:p.Gln863=
ENST00000358913.9:c.3412C=	ENSP00000351790.5:p.Gln1138=
ENST00000540630.5:c.3412C=	ENSP00000441668.2:p.Gln1138=
ENST00000540630.6:c.3466C=	ENSP00000441668.3:p.Gln1156=
ENST00000613327.4:c.2530C=	ENSP00000480757.1:p.Gln844=
ENST00000613327.5:c.3412C=	ENSP00000480757.2:p.Gln1138=
ENST00000688812.1:c.*675C=	ENSP00000510658.1:n.*675C=
ENST00000690544.1:c.*2683C=	ENSP00000508989.1:n.*2683C=
XM_006718043.2:c.3466C=	XP_006718106.1:p.Gln1156=
XM_011540292.1:c.3442C=	XP_011538594.1:p.Gln1148=
XM_017016833.1:c.3490C=	XP_016872322.1:p.Gln1164=
XM_017016834.2:c.3412C=	XP_016872323.1:p.Gln1138=
XM_024448236.1:c.2290C=	XP_024304004.1:p.Gln764=
XR_946029.1:n.1804-219G=